Bansal V - Search Results

1

The diploid genome sequence of an individual human.

Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, Axelrod N, Huang J, Kirkness EF, Denisov G, Lin Y, MacDonald JR, Pang AW, Shago M, Stockwell TB, Tsiamouri A, Bafna V, Bansal V, Kravitz SA, Busam DA, Beeson KY, McIntosh TC, Remington KA, Abril JF, Gill J, Borman J, Rogers YH, Frazier ME, Scherer SW, Strausberg RL, Venter JC. Levy S, et al. Among authors: bansal v. PLoS Biol. 2007 Sep 4;5(10):e254. doi: 10.1371/journal.pbio.0050254. PLoS Biol. 2007. PMID: 17803354 Free PMC article.

2

Inference about recombination from haplotype data: lower bounds and recombination hotspots.

Bafna V, Bansal V. Bafna V, et al. Among authors: bansal v. J Comput Biol. 2006 Mar;13(2):501-21. doi: 10.1089/cmb.2006.13.501. J Comput Biol. 2006. PMID: 16597254

3

The number of recombination events in a sample history: conflict graph and lower bounds.

Bafna V, Bansal V. Bafna V, et al. Among authors: bansal v. IEEE/ACM Trans Comput Biol Bioinform. 2004 Apr-Jun;1(2):78-90. doi: 10.1109/TCBB.2004.23. IEEE/ACM Trans Comput Biol Bioinform. 2004. PMID: 17048383

4

Evidence for large inversion polymorphisms in the human genome from HapMap data.

Bansal V, Bashir A, Bafna V. Bansal V, et al. Genome Res. 2007 Feb;17(2):219-30. doi: 10.1101/gr.5774507. Epub 2006 Dec 21. Genome Res. 2007. PMID: 17185644 Free PMC article.

5

A decomposition theory for phylogenetic networks and incompatible characters.

Gusfield D, Bansal V, Bafna V, Song YS. Gusfield D, et al. Among authors: bansal v. J Comput Biol. 2007 Dec;14(10):1247-72. doi: 10.1089/cmb.2006.0137. J Comput Biol. 2007. PMID: 18047426 Free PMC article.

6

An MCMC algorithm for haplotype assembly from whole-genome sequence data.

Bansal V, Halpern AL, Axelrod N, Bafna V. Bansal V, et al. Genome Res. 2008 Aug;18(8):1336-46. doi: 10.1101/gr.077065.108. Genome Res. 2008. PMID: 18676820 Free PMC article.

7

HapCUT: an efficient and accurate algorithm for the haplotype assembly problem.

Bansal V, Bafna V. Bansal V, et al. Bioinformatics. 2008 Aug 15;24(16):i153-9. doi: 10.1093/bioinformatics/btn298. Bioinformatics. 2008. PMID: 18689818

8

Designing deep sequencing experiments: detecting structural variation and estimating transcript abundance.

Bashir A, Bansal V, Bafna V. Bashir A, et al. Among authors: bansal v. BMC Genomics. 2010 Jun 18;11:385. doi: 10.1186/1471-2164-11-385. BMC Genomics. 2010. PMID: 20565853 Free PMC article.

9

A covering method for detecting genetic associations between rare variants and common phenotypes.

Bhatia G, Bansal V, Harismendy O, Schork NJ, Topol EJ, Frazer K, Bafna V. Bhatia G, et al. Among authors: bansal v. PLoS Comput Biol. 2010 Oct 14;6(10):e1000954. doi: 10.1371/journal.pcbi.1000954. PLoS Comput Biol. 2010. PMID: 20976246 Free PMC article.

10

Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level.

Harismendy O, Bansal V, Bhatia G, Nakano M, Scott M, Wang X, Dib C, Turlotte E, Sipe JC, Murray SS, Deleuze JF, Bafna V, Topol EJ, Frazer KA. Harismendy O, et al. Among authors: bansal v. Genome Biol. 2010;11(11):R118. doi: 10.1186/gb-2010-11-11-r118. Epub 2010 Nov 30. Genome Biol. 2010. PMID: 21118518 Free PMC article.

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